Biomaterial Database

Hospital's independent responsibility to obtain informed consent. 1994

D B Brushwood

UI	MeSH Term	Description	Entries
D007258	Informed Consent	Voluntary authorization, by a patient or research subject, with full comprehension of the risks involved, for diagnostic or investigative procedures, and for medical and surgical treatment.	Consent, Informed
D007882	Legislation, Hospital	Laws and regulations concerning hospitals, which are proposed for enactment or enacted by a legislative body.	Hospital Legislation,Hospital Legislations,Legislations, Hospital
D008318	Malpractice	Failure of a professional person, a physician or lawyer, to render proper services through reprehensible ignorance or negligence or through criminal intent, especially when injury or loss follows. (Random House Unabridged Dictionary, 2d ed)	Professional Negligence,Negligence,Negligence, Professional,Professional Negligences
D010414	Pennsylvania	State bounded on the north by New York and Lake Erie, on the east by Delaware and New Jersey, on the south by Delaware and Maryland, and on the west by Ohio and West Virginia.
D010820	Physicians	Individuals licensed to practice medicine.	Physician
D002986	Clinical Trials as Topic	Works about pre-planned studies of the safety, efficacy, or optimum dosage schedule (if appropriate) of one or more diagnostic, therapeutic, or prophylactic drugs, devices, or techniques selected according to predetermined criteria of eligibility and observed for predefined evidence of favorable and unfavorable effects. This concept includes clinical trials conducted both in the U.S. and in other countries.	Clinical Trial as Topic
D004864	Equipment and Supplies	Expendable and nonexpendable equipment, supplies, apparatus, and instruments that are used in diagnostic, surgical, therapeutic, scientific, and experimental procedures.	Apparatus and Instruments,Devices,Medical Devices,Device, Medical,Devices, Medical,Equipment,Inventories,Medical Device,Supplies,Device,Instruments and Apparatus,Inventory,Supplies and Equipment
D006801	Humans	Members of the species Homo sapiens.	Homo sapiens,Man (Taxonomy),Human,Man, Modern,Modern Man
D006805	Human Experimentation	The use of humans as investigational subjects.	Human Research Subject Protection,Experimentation, Human
D015507	Drugs, Investigational	Drugs which have received FDA approval for human testing but have yet to be approved for commercial marketing. This includes drugs used for treatment while they still are undergoing clinical trials (Treatment IND). The main heading includes drugs under investigation in foreign countries.	Investigational Drug,Investigational New Drug,Investigational New Drugs,Investigational Drugs,Drug, Investigational,Drug, Investigational New,Drugs, Investigational New,New Drug, Investigational,New Drugs, Investigational

Related Publications

D B Brushwood

Procedure to obtain informed consent of patient.

January 1977, Oregon revised statutes : containing, with some exceptions, the statute laws of Oregon of a general, public and permanent nature ... Oregon,

D B Brushwood

Liability for failure to obtain informed consent.

June 1983, Topics in health record management,

D B Brushwood

How to obtain informed consent for research.

June 2018, Breathe (Sheffield, England),

D B Brushwood

Informed consent: hospitals must obtain informed consent prior to drug testing pregnant patients.

January 2003, The Journal of law, medicine & ethics : a journal of the American Society of Law, Medicine & Ethics,

D B Brushwood

Medical: informed consent--designate health care professionals to obtain informed consent. Final rule.

March 2007, Federal register,